FUKUDA DENSHI MODEL SPIROSIFT 3000— 510(k) K900391

Substantially Equivalent

Fukuda Denshi USA, Inc.

FDA 510(k) clearance K900391 for FUKUDA DENSHI MODEL SPIROSIFT 3000, Substantially Equivalent on 1990-04-10. Applicant: Fukuda Denshi USA, Inc..

Clearance details

Applicant: Fukuda Denshi USA, Inc.
Product code: Code BZG
Advisory panel: Anesthesiology
Date received: 1990-01-26
Decision date: 1990-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redmond, WA, US

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